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Viral Uncoating Is Directional: Exit of the Genomic RNA in a Common Cold Virus Starts with the Poly-(A) Tail at the 3′-End

Upon infection, many RNA viruses reorganize their capsid for release of the genome into the host cell cytosol for replication. Often, this process is triggered by receptor binding and/or by the acidic environment in endosomes. In the genus Enterovirus, which includes more than 150 human rhinovirus (...

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Autores principales: Harutyunyan, Shushan, Kumar, Mohit, Sedivy, Arthur, Subirats, Xavier, Kowalski, Heinrich, Köhler, Gottfried, Blaas, Dieter
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Public Library of Science 2013
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3617019/
https://www.ncbi.nlm.nih.gov/pubmed/23592991
http://dx.doi.org/10.1371/journal.ppat.1003270
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author Harutyunyan, Shushan
Kumar, Mohit
Sedivy, Arthur
Subirats, Xavier
Kowalski, Heinrich
Köhler, Gottfried
Blaas, Dieter
author_facet Harutyunyan, Shushan
Kumar, Mohit
Sedivy, Arthur
Subirats, Xavier
Kowalski, Heinrich
Köhler, Gottfried
Blaas, Dieter
author_sort Harutyunyan, Shushan
collection PubMed
description Upon infection, many RNA viruses reorganize their capsid for release of the genome into the host cell cytosol for replication. Often, this process is triggered by receptor binding and/or by the acidic environment in endosomes. In the genus Enterovirus, which includes more than 150 human rhinovirus (HRV) serotypes causing the common cold, there is persuasive evidence that the viral RNA exits single-stranded through channels formed in the protein shell. We have determined the time-dependent emergence of the RNA ends from HRV2 on incubation of virions at 56°C using hybridization with specific oligonucleotides and detection by fluorescence correlation spectroscopy. We report that psoralen UV crosslinking prevents complete RNA release, allowing for identification of the sequences remaining inside the capsid. We also present the structure of uncoating intermediates in which parts of the RNA are condensed and take the form of a rod that is directed roughly towards a two-fold icosahedral axis, the presumed RNA exit point. Taken together, in contrast to schemes frequently depicted in textbooks and reviews, our findings demonstrate that exit of the RNA starts from the 3′-end. This suggests that packaging also occurs in an ordered manner resulting in the 3′-poly-(A) tail becoming located close to a position of pore formation during conversion of the virion into a subviral particle. This directional genome release may be common to many icosahedral non-enveloped single-stranded RNA viruses.
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spelling pubmed-36170192013-04-16 Viral Uncoating Is Directional: Exit of the Genomic RNA in a Common Cold Virus Starts with the Poly-(A) Tail at the 3′-End Harutyunyan, Shushan Kumar, Mohit Sedivy, Arthur Subirats, Xavier Kowalski, Heinrich Köhler, Gottfried Blaas, Dieter PLoS Pathog Research Article Upon infection, many RNA viruses reorganize their capsid for release of the genome into the host cell cytosol for replication. Often, this process is triggered by receptor binding and/or by the acidic environment in endosomes. In the genus Enterovirus, which includes more than 150 human rhinovirus (HRV) serotypes causing the common cold, there is persuasive evidence that the viral RNA exits single-stranded through channels formed in the protein shell. We have determined the time-dependent emergence of the RNA ends from HRV2 on incubation of virions at 56°C using hybridization with specific oligonucleotides and detection by fluorescence correlation spectroscopy. We report that psoralen UV crosslinking prevents complete RNA release, allowing for identification of the sequences remaining inside the capsid. We also present the structure of uncoating intermediates in which parts of the RNA are condensed and take the form of a rod that is directed roughly towards a two-fold icosahedral axis, the presumed RNA exit point. Taken together, in contrast to schemes frequently depicted in textbooks and reviews, our findings demonstrate that exit of the RNA starts from the 3′-end. This suggests that packaging also occurs in an ordered manner resulting in the 3′-poly-(A) tail becoming located close to a position of pore formation during conversion of the virion into a subviral particle. This directional genome release may be common to many icosahedral non-enveloped single-stranded RNA viruses. Public Library of Science 2013-04-04 /pmc/articles/PMC3617019/ /pubmed/23592991 http://dx.doi.org/10.1371/journal.ppat.1003270 Text en © 2013 Harutyunyan et al http://creativecommons.org/licenses/by/4.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are properly credited.
spellingShingle Research Article
Harutyunyan, Shushan
Kumar, Mohit
Sedivy, Arthur
Subirats, Xavier
Kowalski, Heinrich
Köhler, Gottfried
Blaas, Dieter
Viral Uncoating Is Directional: Exit of the Genomic RNA in a Common Cold Virus Starts with the Poly-(A) Tail at the 3′-End
title Viral Uncoating Is Directional: Exit of the Genomic RNA in a Common Cold Virus Starts with the Poly-(A) Tail at the 3′-End
title_full Viral Uncoating Is Directional: Exit of the Genomic RNA in a Common Cold Virus Starts with the Poly-(A) Tail at the 3′-End
title_fullStr Viral Uncoating Is Directional: Exit of the Genomic RNA in a Common Cold Virus Starts with the Poly-(A) Tail at the 3′-End
title_full_unstemmed Viral Uncoating Is Directional: Exit of the Genomic RNA in a Common Cold Virus Starts with the Poly-(A) Tail at the 3′-End
title_short Viral Uncoating Is Directional: Exit of the Genomic RNA in a Common Cold Virus Starts with the Poly-(A) Tail at the 3′-End
title_sort viral uncoating is directional: exit of the genomic rna in a common cold virus starts with the poly-(a) tail at the 3′-end
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3617019/
https://www.ncbi.nlm.nih.gov/pubmed/23592991
http://dx.doi.org/10.1371/journal.ppat.1003270
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